A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037822



Internal ID18780353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75468606..75633843hg38UCSC Ensembl
Innerchr14:75935309..76100186hg19UCSC Ensembl
Innerchr14:75005062..75169939hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38165238
hg19164878
hg18164878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531203
Samples
Known GenesBATF, FLVCR2, JDP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037822
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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